The EMS Sleep Health Study: A Randomized Controlled Trial

University of Pittsburgh

Status: Terminated

Conditions: Sleep Quality; Fatigue

Treatments: Other: Sleep Health Education

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT04218279

DTNH2215R00029 (Other Grant/Funding Number)

STUDY19080090

Details and patient eligibility

About

The experiment seeks to determine the impact of a sleep health and fatigue education and training program on diverse indicators of sleep and fatigue among Emergency Medical Services (EMS) personnel. The overarching goals of this research study are to [1] enhance our understanding of the relationships between shift work, sleep, and fatigue in EMS operations; and [2] determine whether or not providing education and training to EMS personnel on the importance of sleep health and dangers of fatigue impact indicators of sleep and fatigue. The investigators will accomplish these goals by using a cluster-randomized trial study design with a wait-list control group.

Full description

The overarching goals of this research study are to:

1. enhance our understanding of the relationships between shift work, sleep, and fatigue in EMS operations; and
2. determine whether or not providing education and training to EMS personnel on the importance of sleep health and dangers of fatigue impact indicators of sleep and fatigue.

The investigators will recruit EMS nationwide for EMS agencies to participate in this study and focus on moderately sized EMS agencies with between 50 and 300 employees (yet we will not outright exclude smaller or larger organizations). Agencies that run dual ground-based and air-medical EMS services are eligible. Maximum enrollment at the agency-level is n=30 EMS agencies. Agencies will be randomized upon enrollment to one of two arms: [1] Intervention group; or [2] the Wait-List control group. The intervention group will receive immediate access to the intervention materials (the 10 brief Sleep Health Education Modules). The wait-list control group will receive access to intervention materials at 3 months post enrollment/baseline.

Within each agency, the investigators will recruit individual EMS clinicians to participate. Goal enrollment within each agency is a minimum of 30 and a maximum of 50 EMS clinicians.

All individual EMS clinician participants will undergo informed consent, answer a baseline survey, and be queried via mobile phone text message at regular intervals which will begin upon enrollment. These mobile phone text message queries will assess indicators of sleep and fatigue. All participants will be asked to answer two follow up surveys at 3 months and 6 months. The total duration of study participation is 6 months. The primary outcome of interest is sleep quality as measured by the Pittsburgh Sleep Quality Index (PSQI). The secondary outcome of interest is fatigue as measured by the Chalder Fatigue Questionnaire (CFQ).

Enrollment: 678 patients

Sex: All

Ages: 18 to 100 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• EMS Personnel:

  1. 18 years of age or older
  2. Currently working as an EMS clinician
  3. Working a minimum of one shift a week
  4. Working & residing in the United States
  5. Working at one of the EMS organizations that agreed to participate in this study
  6. Have a cellular, mobile, or smart phone that can send and receive text messages
  7. Willing to answer online surveys and respond to text-message queries for seven days in a row every third week of the month for a total of 24 weeks/6 months

Exclusion criteria

• EMS Personnel:

  1. Individuals <18 years of age
  2. Not currently working as an EMS clinician
  3. Does not work a minimum of one shift a week
  4. Does not work and/reside in the United States
  5. Does not work at one of the EMS organizations that agreed to participate in this study
  6. Does not have a cellular, mobile, or smart phone that can send and receive text messages
  7. Is not willing to answer online surveys and respond to text-message queries for seven days in a row every third week of the month for a total of 24 weeks/6 months.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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678 participants in 2 patient groups

Sleep Health Education

Experimental group

Description:

At baseline, the experimental group will have immediate access to 10 brief education modules focused on diverse elements of sleep health and fatigue.

Treatment:

Other: Sleep Health Education

Wait List Control

Active Comparator group

Description:

At 3 months after baseline, the wait-list control group will be provided access to the 10 education modules focused on diverse elements of sleep health and fatigue..

Treatment:

Other: Sleep Health Education